Canonical Allele Identifier: CA2067555503
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs767442503
gnomAD v4: 12-120738778-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738778G>C , CM000674.2:g.120738778G>C GRCh38
NC_000012.11:g.121176581G>C , CM000674.1:g.121176581G>C GRCh37
NC_000012.10:g.119660964G>C NCBI36
NG_007991.1:g.18011G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.934-42G>C MANE Select ENSP00000242592.4:n.934-42G>C
ENST00000242592.8:c.934-42G>C ENSP00000242592.4:n.934-42G>C
ENST00000411593.2:c.922-42G>C ENSP00000401045.2:n.922-42G>C
NM_000017.3:c.934-42G>C NP_000008.1:n.934-42G>C
NM_001302554.1:c.922-42G>C NP_001289483.1:n.922-42G>C
NM_000017.4:c.934-42G>C MANE Select NP_000008.1:n.934-42G>C
NM_001302554.2:c.922-42G>C NP_001289483.1:n.922-42G>C
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